Diaphanous-related formin 1

Preferred Label : Diaphanous-related formin 1;

Symbol : DIAPH1;

CISMeF acronym : DIAPH1;

Type : Gene;

Alternative titles and symbols : Diaphanous, drosophila, homolog of, 1; DIA1;

Ensembl ID : ENSG00000131504;

Prefixed ID : *602121;

Details

Origin ID

602121;

UMLS CUI

C1414047;

Automatic exact mappings (from CISMeF team)
- diaphanous related formin 1 [ORDO Gene]
- diaphanous related formin 1 [HGNC gene]
HGNC gene
- diaphanous related formin 1 [HGNC gene]
ORDO concept(s)
- diaphanous related formin 1 [ORDO Gene]
Phenotypes related
- Deafness, autosomal dominant 1, with or without thrombocytopenia [OMIM Phenotype]
- Seizures, cortical blindness, and microcephaly syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- diaphanous related formin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients